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Pilling

FDA UDI

Class I (US FDA UDI)

by Teleflex Incorporated

Identity

Trade Name
PILLING FDA UDI
Generic Name
Intraocular scissors, conventional-hinge, reusable FDA UDI
Device Name
SCI IRIS RIBBON TYPE LG BLDS BLUNT STR FDA UDI
Model / Reference
IPN020293 FDA UDI
Description
SCI IRIS RIBBON TYPE LG BLDS BLUNT STR FDA UDI

Identifiers

Catalog Number
P24639 FDA UDI
Primary DI / UDI-DI
14026704800435 FDA UDI
FDA Product Code
HNF FDA UDI
GMDN Term
Intraocular scissors, conventional-hinge, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
886.4350 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Intraocular scissors, conventional-hinge, reusable

Pilling by Teleflex Incorporated — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Intraocular scissors, conventional-hinge, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Teleflex Incorporated

Sources (1)

  • FDA UDI 431f6f2e-df8c-4e56-bcc2-51944be26113 35 fields · synced Jun 1, 2026